光动力疗法
光热治疗
单线态氧
癌症研究
肿瘤缺氧
肿瘤微环境
生物标志物
热疗
化学
材料科学
纳米技术
肿瘤细胞
医学
放射治疗
氧气
内科学
有机化学
生物化学
作者
Xin Wei,Chi Zhang,Shasha He,Jiaguo Huang,Jingsheng Huang,Si Si Liew,Ziling Zeng,Kanyi Pu
标识
DOI:10.1002/anie.202202966
摘要
Activatable phototheranostics holds promise for precision cancer treatment owing to the "turn-on" signals and therapeutic effects. However, most activatable phototheranostic probes only possess photodynamic therapy (PDT) or photothermal therapy (PTT), which suffer from poor therapeutic efficacy due to deficient cellular oxygen and complex tumor microenvironment. We herein report a dual-locked activatable phototheranostic probe that activates near-infrared fluorescence (NIRF) signals in tumor, triggers PDT in response to a tumor-periphery biomarker, and switches from PDT to PTT upon detecting a tumor-core-hypoxia biomarker. This PDT-PTT auto-regulated probe exhibits complete tumor ablation under the photoirradiation of a single laser source by producing cytotoxic singlet oxygen at the tumor periphery and generating hyperthermia at tumor-core where is too hypoxic for PDT. This dual-locked probe represents a promising molecular design approach toward precise cancer phototheranostics.
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